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Treatment outcome and long-term follow-up of central nervous system germ cell tumor using upfront chemotherapy with subsequent photon or proton radiation therapy: a single tertiary center experience of 127 patients

机译:中枢神经系统生殖细胞肿瘤的治疗结果和长期随访使用随后的光子或质子放射治疗:127名患者的单一三级中心经验

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摘要

Abstract Background Central nervous system germ cell tumors (CNS GCTs) are a heterogeneous group of brain tumors, which are more common in Asian countries. There have been different therapeutic strategies in treating germinoma and non-germinomatous germ cell tumors (NGGCT), depending on prognosis. Moreover, long-term follow up should be emphasized due to higher late complication rates. Here, we investigated long-term outcomes and complication profiles of 127 CNS GCT patients who received uniform upfront chemotherapy. Methods We retrospectively evaluated outcomes of CNS GCT patients treated in Seoul National University Children’s Hospital from August 2004 to April 2019. Patients were classified as low risk (LR) or high risk (HR) based on pathologic diagnosis and tumor markers. Most patients received upfront systemic chemotherapy with carboplatin, cyclophosphamide, etoposide, and/or bleomycin, followed by either proton or photon radiation therapy according to patients’ choice. Results The median age at diagnosis was 11.9 (range, 3.8–25.1) years, and 54.3% of patients were LR. Photon and proton radiation therapy were administered to 73.2 and 25.2% of patients, respectively. In both LR and HR groups, there were no significant differences in survival between photon and proton radiation therapy. The 10-year relapse incidences were 9.3 and 5.6% in the LR and HR groups, respectively. All recurrences, except one, were local relapse. Six secondary malignancies occurred; the 10-year incidences of secondary malignancy were 2.2 and 7.6% in the LR and HR groups, respectively. The 10-year overall survival rates were 98.3 ± 1.7 and 91.8 ± 3.9% in the LR and HR groups, respectively. In a subgroup analysis of HR group, pathologically diagnosed NGGCT patients (n = 20) showed worse 10-year EFS (65.9 ± 11.9%, p < 0.001) and OS (77.9 ± 9.8%, p = 0.024) rates compared to other HR patients who were not pathologically diagnosed or were confirmed as germinoma with elevated tumor markers. All mortalities were related to disease progression or secondary malignancy. Conclusion The strategy of treating CNS GCTs with upfront chemotherapy according to risk groups resulted in good clinical outcomes and acceptable relapse incidence. However, further modification in the definition of the HR group is needed to reduce long-term complications.
机译:摘要背景中枢神经系统胚芽细胞肿瘤(CNS GCTS)是一种异质脑肿瘤组,在亚洲国家更常见。在治疗生殖器瘤和非生殖器胚芽细胞肿瘤(NGGCT)时,存在不同的治疗策略,这取决于预后。此外,由于更高的复杂性率,应强调长期随访。在这里,我们研究了127个CNS GCT患者的长期结果和并发症曲线,接受均匀的前期化疗。方法从2004年8月至2019年8月,我们回顾性评估了首尔国家大学儿童医院治疗的CNS GCT患者的结果。基于病理诊断和肿瘤标志物,患者被归类为低风险(LR)或高风险(HR)。大多数患者接受了用卡铂,环磷酰胺,依托泊苷和/或博莱霉素接受的前期全身化疗,然后根据患者的选择,然后是质子或光子放射疗法。结果诊断中位年龄为11.9(范围,3.8-25.1)岁,54.3%的患者是LR。光子和质子放射疗法分别施用至73.2和25.2%的患者。在LR和HR组中,光子和质子放射治疗之间的存活率没有显着差异。 10年的复发事件分别为LR和HR组的9.3%和5.6%。除了一个外,所有复发都是当地复发。发生了六次继发性恶性肿瘤; 10年的次要恶性肿瘤发生率分别为LR和HR组中的2.2%和7.6%。 LR和HR组的10年总生存率分别为98.3±1.7和91.8±3.9%。在HR组的子组分析,病理诊断NGGCT患者(n = 20)显示出更差的10年EFS(65.9±11.9%,P <0.001)和OS(77.9±9.8%,p值= 0.024)速率相比其他HR患者谁没有病理诊断或证实与肿瘤标记物升高生殖。所有的死亡率都与疾病进展或继发性恶性有关。结论根据风险群体治疗UNTONT化疗的CNS GCT策略导致了良好的临床结果和可接受的复发发病率。然而,需要在HR组的定义中进行进一步修改以减少长期并发症。

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